COMFY SERIES: EV-804, EV-805 & EV-806— 510(k) K071951

Name: FDA 510(k) clearance K071951
Creator: U.S. Food and Drug Administration
Published: 2007-09-05

Substantially Equivalent

Everyway Medical Instruments Co.,Ltd

FDA 510(k) clearance K071951 for COMFY SERIES: EV-804, EV-805 & EV-806, Substantially Equivalent on 2007-09-05. Applicant: Everyway Medical Instruments Co.,Ltd. Device class: 2.

Clearance details

Applicant: Everyway Medical Instruments Co.,Ltd
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2007-07-16
Decision date: 2007-09-05
Decision: Substantially Equivalent
Clearance type: Special
Location: Roswell, GA, US

Download summary PDF View on FDA.gov ↗

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